The radiocarbon budget for Mono Lake: an unsolved mystery

Since 1957 the ¹⁴C/C ratio of the dissolved inorganic carbon in Mono Lake has risen by about 60‰. The magnitude of this increase is about four times larger than that expected from the invasion of bomb-produced¹⁴C from the atmosphere. We have eliminated the following explanations: (1) measurement error, (2) an unusually high physical exchange rate for non-reactive gases, (3) inorganic enhancement of the CO₂ exchange rate, and (4) biological enhancement of the CO₂ exchange rate. Clandestine disposal of waste radiocarbon remains a dark-horse explanation.In the course of our investigations we have uncovered evidence for at least one episodic input of radiocarbon-free carbon to the lake over the last 1000 years. We speculate that this injection was related to a hydrothermal event resulting from sublacustrine volcanic activity.     

Tidally oscillating bisulfide fluxes and fluid flow rates observed with in situ chemical sensors at a warm spring in Monterey Bay,California

An In Situ Ultraviolet Spectrophotometer (ISUS) was coupled to a benthic chamber to characterize the bisulfide flux emanating from a warm spring at the Extrovert Cliff locality within Monterey Bay, California. The chamber was periodically flushed with bottom seawater to reset chemical concentrations, which enabled deployments over multiple days. Data from several deployments, each lasting at least 10 days, were used to calculate flow rates, fluid concentrations, and fluxes over time. The bisulfide concentration of the fluid entering the chamber varied from 75 to 4500 μmol l^?1. Positive temperature anomalies up to 3.5° were associated with these elevated concentrations. Linear flow rates ranged from 2 to >17 m day^?1, while the bisulfide fluxes varied from 0.2 to 80 mol m^?2 day^?1. The bisulfide originated at depth and was not produced in the surface sediments via an anaerobic oxidation of methane coupled to sulfate reduction. Tides modulated the flow as well as the composition of the fluid entering the chamber. It appeared that a deep sourced fluid, which supplied the bisulfide, was mixed with a second, ambient seawater-like fluid before entering the flux chamber. At low tides, flow rates were at their highest and the contribution of the deep sourced fluid to the fluid entering the chamber was at a maximum.     

Oxidative dissolution potential of biogenic and abiogenic TcO2 in subsurface sediments

Technetium-99 (Tc) is an important fission product contaminant associated with sites of nuclear fuels reprocessing and geologic nuclear waste disposal. Tc is highly mobile in its most oxidized state and less mobile in the reduced form [Tc(IV)O₂·nH₂O]. Here we investigate the potential for oxidation of Tc(IV) that was heterogeneously reduced by reaction with biogenic Fe(II) in two sediments differing in mineralogy and aggregation state; unconsolidated Pliocene-age fluvial sediment from the upper Ringold (RG) Formation at the Hanford Site and a clay-rich saprolite from the Field Research Center (FRC) background site on the Oak Ridge Site. Both sediments contained Fe(III) and Mn(III/IV) as redox active phases, but FRC also contained mass-dominant Fe-phyllosilicates of different types. Shewanella putrefaciens CN32 reduced Mn(III/IV) oxides and generated Fe(II) that was reactive with Tc(VII) in heat-killed, bioreduced sediment. After bioreduction and heat-killing, biogenic Fe(II) in the FRC exceeded that in RG by a factor of two. More rapid reduction rates were observed in the RG that had lower biogenic Fe(II), and less particle aggregation. EXAFS measurements indicated that the primary reduction product was a TcO₂-like phase in both sediments. The biogenic redox product Tc(IV) oxidized rapidly and completely in RG when contacted with air. Oxidation, in contrast, was slow and incomplete in the FRC, in spite of similar molecular scale speciation of Tc compared to RG. X-ray microprobe, electron microprobe, X-ray absorption spectroscopy, and micro X-ray diffraction were applied to the whole sediment and isolated Tc-containing particles. These analyses revealed that non-oxidizable Tc(IV) in the FRC existed as complexes with octahedral Fe(III) within intra-grain domains of 50-100 μm-sized, Fe-containing micas presumptively identified as celadonite. The markedly slower oxidation rates in FRC as compared to RG were attributed to mass-transfer-limited migration of O₂ into intra-aggregate and intraparticle domains where Tc(IV) existed; and the formation of unique, oxidation-resistant, intragrain Tc(IV)-Fe(III) molecular species.     

Mercury emission from terrestrial background surfaces in the eastern USA. II: Air/surface exchange of mercury within forests from South Carolina to New England

Mercury air/surface exchange was measured over litter-covered soils with low Hg concentrations within various types of forests along the eastern seaboard of the USA. The fieldwork was conducted at six forested sites in state parks in South Carolina, North Carolina, New Jersey, Pennsylvania, New York and Maine from mid-May to early June 2005. The study showed that the Hg air/surface exchange was consistently very low and similar (overall daytime mean flux = 0.2 ± 0.9 ng m⁻² h⁻¹, n = 310, for all six sites monitored) with the various forest types. These flux values are comparable with those found in a year-long study in Tennessee (yearly daytime mean = 0.4 ± 0.5 ng m⁻² h⁻¹), but lower than many previous flux results reported for background soils. The Hg fluxes at all sites oscillated around zero, with many episodes of deposition (negative fluxes) occurring in both daytime and nighttime. While there were particular days showing significant correlations among the Hg air/surface exchange and certain environmental parameters, perhaps because of the low fluxes encountered, few significant correlations were found for any particular day of sampling between the Hg flux and environmental parameters such as solar radiation, soil temperature, air temperature (little variability seen), relative humidity, and ambient air Hg concentrations. Factors driving the Hg exchange as previously found for enriched soils may not hold for these background litter-covered forest soils. The results suggest that spatial variations of the Hg air/surface exchange were small among these different forest types for this particular time of year.     

A Holocene pollen record of persistent droughts from Pyramid Lake, Nevada, USA

Pollen and algae microfossils preserved in sediments from Pyramid Lake, Nevada, provide evidence for periods of persistent drought during the Holocene age. We analyzed one hundred nineteen 1-cm-thick samples for pollen and algae from a set of cores that span the past 7630 years. The early middle Holocene, 7600 to 6300 cal yr B.P., was found to be the driest period, although it included one short but intense wet phase. We suggest that Lake Tahoe was below its rim for most of this period, greatly reducing the volume and depth of Pyramid Lake. Middle Holocene aridity eased between 5000 and 3500 cal yr B.P. and climate became variable with distinct wet and dry phases. Lake Tahoe probably spilled intermittently during this time. No core was recovered that represented the period between 3500 and 2600 cal yr B.P. The past 2500 years appear to have had recurrent persistent droughts. The timing and magnitude of droughts identified in the pollen record compares favorably with previously published δ¹⁸O data from Pyramid Lake. The timing of these droughts also agrees with the ages of submerged rooted stumps in the Eastern Sierra Nevada and woodrat midden data from central Nevada. Prolonged drought episodes appear to correspond with the timing of ice drift minima (solar maxima) identified from North Atlantic marine sediments, suggesting that changes in solar irradiance may be a possible mechanism influencing century-scale drought in the western Great Basin.     

Exploring fishing dependence in gulf coast communities

Two unrelated data sources (quantitative secondary data and qualitative primary data) and mixed methodologies (statistical analysis and ethnography) are used to define the concept of, and develop indicators for, fishing dependence. Techniques for integrating differing data sources are developed. Comparisons of the qualitative rankings with the quantitative rankings were, overall, positive and statistically significant. The process used thus confirmed that the indicators were reliable measures for fishing dependence. In terms of external validity and triangulation, the process used was more rigorous than using ethnography “after-the-fact” to ground-truth the quantitative indicators.